De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair

H. Hampel,; C.M. Allen,; S.D. Chernausek,; T.W. Prior,; C. Eng,

doi:10.1515/IJDHD.2000.1.3.143

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De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair

H. Hampel, , C.M. Allen, , S.D. Chernausek, , T.W. Prior, und C. Eng,

Veröffentlicht/Copyright: 1. Juli 2000

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Aus der Zeitschrift International Journal on Disability and Human Development Band 1 Heft 3

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Hampel,, H., Allen,, C.M., Chernausek,, S.D., Prior,, T.W. and Eng,, C.. "De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair" International Journal on Disability and Human Development, vol. 1, no. 3, pp. 143-148. https://doi.org/10.1515/IJDHD.2000.1.3.143

Hampel,, H., Allen,, C., Chernausek,, S., Prior,, T. & Eng,, C. (). De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair. International Journal on Disability and Human Development, 1(3), 143-148. https://doi.org/10.1515/IJDHD.2000.1.3.143

Hampel,, H., Allen,, C., Chernausek,, S., Prior,, T. and Eng,, C. () De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair. International Journal on Disability and Human Development, Vol. 1 (Issue 3), pp. 143-148. https://doi.org/10.1515/IJDHD.2000.1.3.143

Hampel,, H., Allen,, C.M., Chernausek,, S.D., Prior,, T.W. and Eng,, C.. "De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair" International Journal on Disability and Human Development 1, no. 3 (): 143-148. https://doi.org/10.1515/IJDHD.2000.1.3.143

Hampel, H, Allen, C, Chernausek, S, Prior, T, Eng, C. De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair. International Journal on Disability and Human Development. ;1(3): 143-148. https://doi.org/10.1515/IJDHD.2000.1.3.143

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Published Online: 2000-07

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Letter from the Editors
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Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene
Novel Mutation (Arg836ter) of the Sulfonylurea Receptor-1 (SUR1) Gene in Congenital Hyperinsulinism
De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair
Bromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 Gene
Genetic Studies in Familial Aldosteronism Not Suppressible by Dexamethasone
Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred
BOOK REVIEWS. CALENDAR

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https://doi.org/10.1515/IJDHD.2000.1.3.143

Artikel in diesem Heft

CONTENTS
Letter from the Editors
Prader-Willi and Angelman Syndromes: Diagnostic Approach
Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene
Novel Mutation (Arg836ter) of the Sulfonylurea Receptor-1 (SUR1) Gene in Congenital Hyperinsulinism
De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair
Bromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 Gene
Genetic Studies in Familial Aldosteronism Not Suppressible by Dexamethasone
Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred
BOOK REVIEWS. CALENDAR